Substantially homogeneous copolymers of vinyl pyrrolidone and N-3,3-dimethylaminopropyl methacrylamide for personal care applications

ABSTRACT

Substantially homogeneous copolymers comprising 20-99% of vinyl pyrrolidone (VP) and 1-80% of N-3,3-dimethylaminopropyl methacrylamide, (DMAPMA), preferably 50-95% VP and 5-50% DMAPMA, and, most preferably, about 80:20, by weight, having a weight average molecular weight of about 200,000 to 1,500,000, as a clear, low viscosity aqueous solution of the homogeneous copolymer, at a 5-20% solids level, preferably about 10-15%, by weight of the solution, having a viscosity of about 5,000 to 80,000 cps, preferably about 10,000 to 70,000 cps. The solution obtained herein has lower viscosity and better clarity, and provides hair care products with enhanced curl retention (hold), when compared to non-homogeneous copolymers of the same composition, or related existing commercial products.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a process for making substantially homogeneouscopolymers of vinyl pyrrolidone (VP) and N-3,3-dimethylaminopropylmethacrylamide (DMAPMA) of predetermined composition and clear, lowviscosity aqueous solutions thereof, for use in hair styling and haircare applications.

2. Description of the Prior Art

Several synthetic polymers containing vinyl lactams are presently beingused in cosmetic formulations, particularly in hair care products, tocontribute body, set retention and conditioning to such products.

Representative of the art in this field are the following U.S. Pat.Nos.: 3,914,403; 3,954,960; 4,057,533; 4,210,161; 4,586,518; 4,753,793;4,764,363; 4,834,968; 4,842,850; 4,902,499; 4,906,459; 4,923,694;4,963,348; 4,983,377; 5,011,895 and 5,015,708; and WO 91/15186; WO91/15185; EPO 0412704A2; EPO 0412707A1; and JP 57126409.

Generally these synthetic polymers were made by a "one-pot"polymerization process in which selected amounts of the several monomerswere reacted together. The composition of these one-pot polymers wasconsidered as being the same as the composition of the charged monomers.However, in reality, such a polymerization process can provide only amixture of polymers of various compositions, and, additionally, anindeterminate amount of homopolymers and undesired copolymers.

Accordingly, it is an object of this invention to provide a process formaking substantially homogeneous copolymers of vinyl pyrrolidone (VP)and N-3,3-dimethylaminopropyl methacrylamide (DMAPMA).

Another object of this invention is to provide a clear, low viscosityaqueous solution of homogeneous copolymers of VP and DMAPMA, in acompositional range of 20-99% VP and 1-80% DMAPMA, preferably 50-95% VPand 5-50% DMAPMA, and most preferably about 80% VP and 20% DMAPMA, at asolids level of 5-20%, preferably about 10-15%, by weight of thesolution, having a viscosity of about 5,000 to 80,000 cps, preferablyabout 10,000 to 70,000 cps.

Still another object herein is to provide clear, low viscosity aqueoussolutions of substantially homogeneous copolymers of VP and DMAPMA in apredetermined compositional range and at a selected solids level, which,upon formulation into hair styling compositions, will provide enhancedconditioning, fixative and hair holding properties for the user.

SUMMARY OF THE INVENTION

A process is described herein for making substantially homogeneouscopolymers of 20-99% vinyl pyrrolidone and 1-80%N-3,3-dimethylaminopropyl methacrylamide, preferably about 50-95% VP and5-50% DMAPMA, and most preferably about 80% VP and 20% DMAPMA, byweight, having a weight average molecular weight of about 200,000 to1,500,000, and a clear, low viscosity aqueous solution of-thehomogeneous copolymer at a 5-20% solids level, preferably about 10-15%,by weight of the solution, and having a viscosity of about 5,000 to80,000 cps, preferably about 10,000 to 70,000 cps.

The copolymer solution obtained herein is less viscous and has betterclarity than solutions of non-homogeneous copolymers of the samecomposition, or of related commercial products. When formulated intohair styling compositions, these homogeneous polymer solutions alsoprovide improved curl retention (hold) during use.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graphical representation of a non-homogeneous (one-pot)process in which is plotted percent unreacted VP and DMAPMA vs. time fora reaction mixture of 80:20% by weight VP/DMAPMA copolymer at 15%solids.

FIG. 2 is a graphical representation of the homogeneous process of theinvention in which is plotted percent unreacted VP and DMAPMA vs. timeduring the preparation of an aqueous solution of 80:20% by weightVP/DMAPMA copolymer at 15% solids.

DETAILED DESCRIPTION OF THE INVENTION

In accordance with the present invention, a process is provided formaking substantially homogeneous copolymers of vinyl pyrrolidone andN-3,3-dimethylaminopropyl methacrylamide of predetermined composition.

In this process, the less reactive monomer of the copolymer (VP) isprecharged into a reactor at a suitable reaction temperature, generallyabout 50°-80° C., preferably 55°-75° C. Then the more reactive monomer(DMAPMA) is introduced incrementally into the VP-charged reactor at arate which corresponds to the observed rate of disappearance of VP.

The entire predetermined amount of the DMAPMA monomer is added beforesubstantially all the VP monomer has been consumed so that both monomerscan react to form a substantially homogeneous copolymer in a desiredcompositional ratio of VP:DMAPMA. Consequently, a copolymer is obtainedwhose composition approaches the nominal monomer ratio of the desiredcopolymer composition and whose structure has the two individualmonomeric units of the copolymer distributed substantially uniformly ina homogeneous chain along the backbone of the polymer. For example, foran 80:20 weight ratio of VP/DMAPMA copolymer, which is approximatelyequivalent to a 6:1 mole ratio of VP/DMAPMA, the homogeneous copolymerof the invention has a monomer distribution corresponding substantiallyclose to VP-VP-VP-VP-VP-VP-DMAPMA-VP-VP-VP-VP-VP-VP-DMAPMA . . .

The precharge in the process of the invention may include some DMAPMAtherein, generally in an amount which is less than 10% of the totalamount of DMAPMA required for the predetermined copolymer compositionwithout affecting the homogeneous polymerization process. However, it isstill necessary that the rate of addition of DMAPMA after any prechargeis carried out at substantially the rate of disappearance of VP duringcopolymerization.

The schedule of addition of DMAPMA to accomplish the desired matchedrate of reaction of VP is determined in the following manner.

DETERMINATION OF ADDITION SCHEDULE FOR DMAPMA TO FORM A HOMOGENEOUSCOPOLYMER OF VP AND DMAPMA

A. First, a one-pot copolymerization of VP and DMAPMA was carried out asfollows:

EXAMPLE 1

VP (215 g), DMAPMA (54 g), and deionized water (1530 g) were chargedinto a 2-liter resin pot equipped with a gas inlet, a liquid inlet, athermometer and a condenser. A stream of nitrogen then was bubbledthrough the solution and maintained during the reaction. The solutionwas gradually heated to 68° C.; then 0.25 ml of Lupersol 11(t-butylperoxy pivalate) as catalyst was added; then another 0.25 ml ofthe catalyst was added after 10 minutes; and another 6 units of 0.25 mlwas added each 30 minutes. The total addition was carried out over a4-hour period.

The relative percentage amounts of residual monomers present during thecourse of the one-pot reaction was determined by gas chromatographicanalysis after sampling the reaction mixture periodically. Theanalytical data obtained then was plotted as the graph of FIG. 1.

As shown in FIG. 1, DMAPMA reacts much more rapidly than VP.Accordingly, after 240 minutes, all the DMAPMA is consumed whileresidual VP monomer still is available for homopolymerization. Thus thecopolymer formed is of a composition different from the desired monomerratio selected by the precharged amounts of the two monomers. Underthese experimental conditions, the polymer product obtained is a complexmixture of a homopolymer which is polyvinylpyrrolidone, and a copolymerof VP and DMAPMA of uncertain composition.

B. To form a homogeneous copolymer, it is necessary that the curve ofrate of reaction vs. time for DMAPMA substantially coincide or match therate of reaction curve for VP. To accomplish this, the VP is prechargedand substantially all the DMAPMA is fed after to the precharge at afeeding schedule determined by analysis of the data of FIG. 1. The %DMAPMA monomer to be fed at time t of the polymerization is determinedfrom the Asymmetric Double Sigmoidal Distribution formula, A_(t), below,which has four adjustable parameters, a₁, a₂, a₃ and a₄ : ##EQU1## wheret=time in minutes during copolymerization;

a₁ is a parameter which determines the center of the distribution;

a₂ is a parameter which affects the width of the distribution;

a₃ is a parameter which determines the ascending portion of thedistribution; and

a₄ is a parameter which determines the descending portion of thedistribution. ##EQU2## where N=time when the polymerization iscompleted.

To match the DMAPMA curve to the VP curve of FIG. 1, an "initial guess"is made for the values of a₁, a₂, a₃ and a₄. These values are insertedinto the A_(t) formula and the % DMAPMA to be fed at time t iscalculated. Then a polymerization reaction is carried out using thisschedule. The resulting % unreacted DMAPMA during this polymerizationwill probably not match the % unreacted VP at the same time t. If the %unreacted DMAPMA at time t is too large, then the value of a₃(ascendency) in the A_(t) formula is increased, a₄ (descendency) isdecreased, a₁ (center) is decreased, and a₂ (width) is decreased.Conversely, if the initial guess values of a₁ through a₄ give a reactionrate for DMAPMA which is too fast, then changes in the values of a₁through a₄ are made in a direction opposite to those discussed above.

These new values of the parameters are then used to determine a newfeeding schedule. Using this feeding schedule, another polymerization iscarried out, and the process of adjustment of the parameters describedabove is repeated.

This process is known as "interative fitting" of data to a curve. After4 or 5 such iterative fittings, the experimental VP and DMAPMA curveswill be matched to a satisfactory degree, as shown in FIG. 2 herein.

The matching curve of DMAPMA in FIG. 2 can originate from at least oneset of values for a₁, a₂, a₃ and a₄ (the last set of the iterativefitting process) used to calculate a suitable feeding schedule of DMAPMAover the entire period of the polymerization. One such set is:

a₁ =17

a₂ =28

a₃ =2

a₄ =40

C. With such a suitable DMAPMA feeding schedule available, a homogeneouscopolymer of VP and DMAPMA was prepared as described in Example 2 below.

EXAMPLE 2 Preparation of a Homogeneous Copolymer of VP and DMAPMA

In this example, residual monomers were monitored as in Example 1.

In this process, 216 grams of vinylpyrrolidone (recrystallized material)and 580 grams of deionized water were charged to a 2-liter waterjacketed resin flask.

The flask was equipped with an overhead stirrer connected to an anchorstirrer, a nitrogen inlet for sparging to remove dissolved air and athermocouple which is connected to a temperature controller. Thetemperature was raised to 68° C., by passing heated water from atemperature controlled bath into the jacket of the resin flask. Amechanical syringe pump which could be set to deliver DMAPMA at a setrate was connected to the reactor through polyethylene tubing.

The DMAPMA reactant was added from the syringe pump as a 1 litersolution of 54 grams of DMAPMA in water, according to the followingfeeding schedule:

    ______________________________________                                        Time        Amount of DMAPMA                                                  (min.)      Solution Added (ml)                                               ______________________________________                                         0-30       418.58                                                            30-60       269.80                                                            60-90       153.90                                                             90-120     80.56                                                             120-150     40.10                                                             150-180     19.38                                                             180-210     9.32                                                              210-240     4.38                                                              ______________________________________                                    

The totals added during the entire reaction were VP (216 grams), DMAPMA(54 grams) and water (1530 grams).

Additions of Lupersol 11 (t-butyl peroxypivalate, Atochem, NA) initiatorwere made at various intervals throughout the initial part of thereaction. Additions of 0.25 ml of the initiator were made at 0, 10, 40,70, 100, 140 and 180 minutes. At 210 and 240 minutes, 0.25 ml of eitherVAZO 501 (4,4'-azobis(4-cyanovaleric) acid, Wako Pure ChemicalIndustries, Ltd, Japan) was added to complete the reaction of anyresidual vinylpyrrolidone monomer. For this purpose, the reaction wasallowed to proceed for a total of 10 hours. During this final period thetemperature was raised to 75° C. where it was maintained until thereaction was completed.

The product was discharged as a clear, moderately viscous, aqueoussolution of a substantially homogeneous copolymer of VP and DMAPMA in an80:20 weight ratio at a 15% solids level. The residual vinylpyrrolidonecontent was <0.1%.

The procedure described above can be repeated to provide optimizedDMAPMA feeding schedules for any selected copolymer composition, and atany particular solids content, at a prescribed polymerizationtemperature, solvent level, and amount of initiator.

Table 1 below shows the advantageous physical properties of lowviscosity and enhanced clarity for the homogeneous copolymer solution ofthe invention, as compared to non-homogeneous copolymer solutions of thesame composition.

                  TABLE 1                                                         ______________________________________                                                 Viscosity***                                                                              Clarity.sup.+                                                     (cps)       (NTU)    Mol. Wt.                                        ______________________________________                                        Homogeneous                                                                               61,500       1.80*    610,000                                     copolymer                                                                     solution                                                                      Non-homogeneous                                                                          150,000       14.15**  620,000                                     copolymer                                                                     solution                                                                      ______________________________________                                         .sup.+ Hach; on 0.4% aqueous solution                                         *pH = 7.98                                                                    **pH = 7.44                                                                   ***Brookfield viscosity, on 15% aqueous solution; Model RTV, 20 rpm,          Spindle #7, 25° C.                                                

HAIR STYLING COMPOSITIONS

The substantially homogeneous copolymer of the invention findsparticular utility in multifunctional hair care products such aswater-based, rinse-off hair styling and conditioning products, and inmousse hair care products. It may be included in such compositions as aconcentrate, or as a gel, and applied as a self-actuated pump hairspray, or in an aerosol product with a propellant. Various actuator andpackaging devices known in the art may be used therewith.

Such hair styling products have significantly improved hair holding(curl retention) and hair stiffness properties, while maintainingenhanced hair conditioning (detangling, flyaway and combability)properties, compared to non-homogeneously prepared copolymers of thesame monomers, when formulated into hair styling compositions.

HAIR STYLING COMPOSITIONS OF INVENTION

    ______________________________________                                        Hair Styling Gel           Wt (g)                                             ______________________________________                                        (a)   Homogeneous copolymer of VP/DMAPMA                                                                     5.00                                                 (80:20) (as 15% aqueous solution)                                       (b)   Hydroxyethyl cellulose (Natrosol ®                                                                 0.50                                                 250 HHR-Aqulon)                                                         (c)   Triethanolamine (99%) (TEA)                                                                            0.20                                           (d)   Deionized water          qs                                             ______________________________________                                    

Preparation

1. Heat (d) to 85° C.

2. Add (b) while mixing well.

3. Add (a) with rapid mixing.

4. Neutralize with (c).

    ______________________________________                                        Hair Styling Mousse        Wt (g)                                             ______________________________________                                        (a)   Homogeneous copolymer of VP/DMAPMA                                                                     5.0                                                  (80:20) (as 15% aqueous solution)                                       (b)   Sodium cocoyl isothionate                                                                              0.75                                                 (Igepon ® AC-78 Rhone-Poulenc)                                      (c)   Emulsifying wax (Polowax ® A-31 Croda)                                                             0.15                                           (d)   Propylene glycol, diazolidinyl                                                                         0.25                                                 urea, methyl paraben and propyl                                               paraben (Germaben ® II - Sutton (ISP)                               (e)   Dymel ® 152A (1,1-difluoroethane)                                                                  4.00                                           (f)   Hydrocarbon A-17 (n-butane)                                                                            4.00                                           (g)   Water                    qs                                             ______________________________________                                    

Preparation

1. Add (a) to (g) while agitating and heating to 55°-60° C.

2. Add (b) while mixing at 55° C. Begin cooling.

3. Add (c) and mix rapidly.

4. Cool to 25° C. and add (d).

5. Charge into pressurized container and add (e) and (f).

Table 2 below demonstrates the advantageous curl retention property fora hair styling composition (gel) containing the homogeneous copolymer ofthe invention as compared to a non-homogeneous copolymer.

                  TABLE 2                                                         ______________________________________                                        CURL RETENTION PROPERTY                                                       ______________________________________                                        Copolymer in Hair  Relative Curl Retention                                    Styling Composition                                                                              of Composition*                                            ______________________________________                                        Homogeneous Copolymer                                                                            116.9                                                      Non-homogeneous Copolymer                                                                         95.3                                                      ______________________________________                                         *vs. standard at 90% RH and 90 min. duration                             

While the invention has been described with particular reference tocertain embodiments thereof, it will be understood that changes andmodifications may be made which are within the skill of the art.Accordingly, it is intended to be bound only by the following claims, inwhich:

What is claimed is:
 1. A clear, aqueous solution of a homogeneouscopolymer of VP and DMAPMA, in the compositional ratio of 20-99% byweight VP and 1-80% by weight DMAPMA, having a weight average molecularweight of about 200,000 to about 1,500,000, a solids content of about5-20%, a Brookfield viscosity of about 10,000 to 80,000 cps, and a Hachclarity of less than about
 2. 2. A clear, aqueous solution according toclaim 1 wherein said compositional ratio is about 50-95% VP to 5-50%DMAPMA.
 3. A clear, aqueous solution according to claim 1 wherein saidsolids content is about 10-15%.
 4. A clear, aqueous solution accordingto claim 3 wherein said viscosity is about 10,000 to 70,000 cps.
 5. Aclear, aqueous solution according to claim 1 wherein said compositionalratio is about 80:20, in % by weight.
 6. The product of the process ofmaking clear, aqueous solutions of a substantially homogeneous copolymerof vinyl pyrrolidone (VP) and N-3,3-dimethylaminopropyl methacrylamide(DMAPMA), in the compositional range of 20-99% VP and 1-80% DMAPMA, byweight, having a weight average molecular weight of about 200,000 toabout 1,500,000, a solids content of about 5-20%, and a viscosity ofabout 5,000 to 80,000 cps, by polymerization of the monomers in water inthe presence of a radical initiator, which comprises:(a) precharging areactor with a predetermined amount of VP, and water, at a suitablepolymerization temperature, and (b) introducing DMAPMA into said reactorat a specified feeding schedule determined by the following Equations 1and 2: ##EQU3## where A_(t) has four adjustable parameters, a₁, a₂, a₃and a₄ ; a₁ is a parameter which determines the center of thedistribution; a₂ is a parameter which affects the width of thedistribution; a₃ is a parameter which determines the ascending portionof the distribution; and a₄ is a parameter which determines thedescending portion of the distribution; and t=time (in minutes) from thebeginning of the copolymerization; ##EQU4## where N=time when thepolymerization is completed; wherein a set of determined values for a₁,a₂, a₃ and a₄ provides said specific feeding schedule for DMAPMA andassures that the curve of the rate of disappearance of the VP, duringthe polymerization is substantially matched by the rate of disappearanceof the DMAPMA monomer, as shown in FIG. 2 herein.